rs7964157
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7964157(C;C) |
Make rs7964157(C;T) |
Make rs7964157(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 12 |
Position | 117544415 |
Gene | KSR2 |
is a | snp |
is | mentioned by |
dbSNP | rs7964157 |
dbSNP (classic) | rs7964157 |
ClinGen | rs7964157 |
ebi | rs7964157 |
HLI | rs7964157 |
Exac | rs7964157 |
Gnomad | rs7964157 |
Varsome | rs7964157 |
LitVar | rs7964157 |
Map | rs7964157 |
PheGenI | rs7964157 |
Biobank | rs7964157 |
1000 genomes | rs7964157 |
hgdp | rs7964157 |
ensembl | rs7964157 |
geneview | rs7964157 |
scholar | rs7964157 |
rs7964157 | |
pharmgkb | rs7964157 |
gwascentral | rs7964157 |
openSNP | rs7964157 |
23andMe | rs7964157 |
SNPshot | rs7964157 |
SNPdbe | rs7964157 |
MSV3d | rs7964157 |
GWAS Ctlg | rs7964157 |
Max Magnitude | 0 |
[PMID 26507551] Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome